JP2017502013A5 - - Google Patents

Download PDF

Info

Publication number
JP2017502013A5
JP2017502013A5 JP2016540553A JP2016540553A JP2017502013A5 JP 2017502013 A5 JP2017502013 A5 JP 2017502013A5 JP 2016540553 A JP2016540553 A JP 2016540553A JP 2016540553 A JP2016540553 A JP 2016540553A JP 2017502013 A5 JP2017502013 A5 JP 2017502013A5
Authority
JP
Japan
Prior art keywords
cas number
inhibitor
delta
cancer
intellikine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP2016540553A
Other languages
English (en)
Japanese (ja)
Other versions
JP6678584B2 (ja
JP2017502013A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2014/071747 external-priority patent/WO2015095840A1/en
Publication of JP2017502013A publication Critical patent/JP2017502013A/ja
Publication of JP2017502013A5 publication Critical patent/JP2017502013A5/ja
Application granted granted Critical
Publication of JP6678584B2 publication Critical patent/JP6678584B2/ja
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2016540553A 2013-12-20 2014-12-19 Cdk阻害剤およびerk阻害剤の組み合わせを使用するがん処置 Active JP6678584B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361919597P 2013-12-20 2013-12-20
US61/919,597 2013-12-20
PCT/US2014/071747 WO2015095840A1 (en) 2013-12-20 2014-12-19 Cancer treatments using combinations of cdk and erk inhibitors

Publications (3)

Publication Number Publication Date
JP2017502013A JP2017502013A (ja) 2017-01-19
JP2017502013A5 true JP2017502013A5 (cg-RX-API-DMAC7.html) 2018-02-01
JP6678584B2 JP6678584B2 (ja) 2020-04-22

Family

ID=53403797

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2016540553A Active JP6678584B2 (ja) 2013-12-20 2014-12-19 Cdk阻害剤およびerk阻害剤の組み合わせを使用するがん処置

Country Status (6)

Country Link
US (5) US11013743B2 (cg-RX-API-DMAC7.html)
EP (2) EP3082423B1 (cg-RX-API-DMAC7.html)
JP (1) JP6678584B2 (cg-RX-API-DMAC7.html)
AU (1) AU2014368927B2 (cg-RX-API-DMAC7.html)
ES (1) ES3033810T3 (cg-RX-API-DMAC7.html)
WO (1) WO2015095840A1 (cg-RX-API-DMAC7.html)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8193182B2 (en) 2008-01-04 2012-06-05 Intellikine, Inc. Substituted isoquinolin-1(2H)-ones, and methods of use thereof
CN104926815B (zh) 2008-01-04 2017-11-03 英特利凯恩有限责任公司 某些化学实体、组合物和方法
AR084824A1 (es) 2011-01-10 2013-06-26 Intellikine Inc Procesos para preparar isoquinolinonas y formas solidas de isoquinolinonas
US8828998B2 (en) 2012-06-25 2014-09-09 Infinity Pharmaceuticals, Inc. Treatment of lupus, fibrotic conditions, and inflammatory myopathies and other disorders using PI3 kinase inhibitors
HRP20181367T4 (hr) 2012-11-01 2021-11-26 Infinity Pharmaceuticals, Inc. Liječenje raka korištenjem modulatora izoforme pi3 kinaze
WO2015160975A2 (en) 2014-04-16 2015-10-22 Infinity Pharmaceuticals, Inc. Combination therapies
WO2017021177A1 (en) * 2015-08-04 2017-02-09 Universitat De Barcelona Pharmaceutical combinations for use in the treatment of cancer
CN108135905A (zh) * 2015-08-28 2018-06-08 诺华股份有限公司 用于治疗癌症的cdk4/6抑制剂lee011、mek1/2抑制剂曲美替尼以及可任选还包括pi3k抑制剂byl719的组合
RU2749025C2 (ru) * 2016-03-24 2021-06-03 Трагара Фармасьютикалз, Инк. Лечение рака при помощи tg02
GB201605126D0 (en) * 2016-03-24 2016-05-11 Univ Nottingham Inhibitors and their uses
CA3028718A1 (en) 2016-06-24 2017-12-28 Infinity Pharmaceuticals, Inc. Combination therapies
WO2018081204A1 (en) * 2016-10-26 2018-05-03 Li George Y DEUTERATED N-(5-((4-ETHYLPIPERAZIN-1-YL)METHYL) PYRIDIN-2-YL)-5-FLUORO-4-(4-FLUORO-1-ISOPROPYL-2-METHYL-1H-BENZO[d]IMIDAZOL-6-YL)PYRIMIDIN-2-AMINE
CA3063614A1 (en) * 2017-05-16 2018-11-22 Biomed Valley Discoveries, Inc. Compositions and methods for treating cancer with atypical braf mutations
WO2018218633A1 (en) * 2017-06-02 2018-12-06 Beijing Percans Oncology Co. Ltd. Combination therapies for treating cancers
JP2019116429A (ja) * 2017-12-26 2019-07-18 国立大学法人名古屋大学 抗ウイルス薬
MY205589A (en) 2018-01-08 2024-10-28 G1 Therapeutics Inc G1t38 superior dosage regimes
KR20200132902A (ko) * 2018-03-13 2020-11-25 보드 오브 리전츠, 더 유니버시티 오브 텍사스 시스템 Egfr 활성화 돌연변이를 갖는 암의 치료 방법
WO2019195959A1 (en) 2018-04-08 2019-10-17 Cothera Biosciences, Inc. Combination therapy for cancers with braf mutation
WO2019199883A1 (en) * 2018-04-09 2019-10-17 G1 Therapeutics, Inc. Treatment of cancers having driving oncogenic mutations
BR112021002622A2 (pt) 2018-08-13 2021-05-11 Beijing Percans Oncology Co. Ltd. biomarcadores para terapia de câncer
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
WO2020168197A1 (en) 2019-02-15 2020-08-20 Incyte Corporation Pyrrolo[2,3-d]pyrimidinone compounds as cdk2 inhibitors
MA54947A (fr) * 2019-02-15 2021-12-22 Incyte Corp Biomarqueurs de kinase 2 dépendant de la cycline et leurs utilisations
WO2020180959A1 (en) 2019-03-05 2020-09-10 Incyte Corporation Pyrazolyl pyrimidinylamine compounds as cdk2 inhibitors
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
US11440914B2 (en) 2019-05-01 2022-09-13 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
PH12022550361A1 (en) 2019-08-14 2023-02-27 Incyte Corp Imidazolyl pyrimidinylamine compounds as cdk2 inhibitors
MX2022004390A (es) 2019-10-11 2022-08-08 Incyte Corp Aminas biciclicas como inhibidores de la cinasa dependiente de ciclina 2 (cdk2).
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors
CN117224545A (zh) * 2023-09-26 2023-12-15 中国人民解放军陆军军医大学第二附属医院 Aminopurvalanol A在制备治疗肺腺癌的药物中的应用
WO2025111447A1 (en) * 2023-11-21 2025-05-30 Florida Atlantic University Board Of Trustees Treatment of cancer with drug combinations

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994021822A1 (en) 1993-03-19 1994-09-29 Sequenom, Inc. Dna sequencing by mass spectrometry via exonuclease degradation
US6140053A (en) 1996-11-06 2000-10-31 Sequenom, Inc. DNA sequencing by mass spectrometry via exonuclease degradation
US7439016B1 (en) 2000-06-15 2008-10-21 Digene Corporation Detection of nucleic acids by type-specific hybrid capture method
US7601497B2 (en) 2000-06-15 2009-10-13 Qiagen Gaithersburg, Inc. Detection of nucleic acids by target-specific hybrid capture method
KR20060111716A (ko) * 2002-01-22 2006-10-27 워너-램버트 캄파니 엘엘씨 2-(피리딘-2-일아미노)-피리도[2,3-d]피리미딘-7-온
US7119200B2 (en) * 2002-09-04 2006-10-10 Schering Corporation Pyrazolopyrimidines as cyclin dependent kinase inhibitors
GB0320059D0 (en) 2003-08-27 2003-10-01 Solexa Ltd A method of sequencing
PT3305776T (pt) * 2004-05-14 2019-12-17 Vertex Pharma Compostos de pirrol como inibidores de proteína quinaseserk e composições farmacêuticas que contêm esses compostos
US7582623B2 (en) 2004-05-20 2009-09-01 The Regents Of The University Of California Photoactive metal nitrosyls for blood pressure regulation and cancer therapy
US20060228721A1 (en) 2005-04-12 2006-10-12 Leamon John H Methods for determining sequence variants using ultra-deep sequencing
RU2475484C2 (ru) * 2007-06-05 2013-02-20 Шеринг Корпорейшн Полициклические производные индазола и их применение в качестве ингибиторов erk для лечения рака
BRPI0917791B1 (pt) * 2008-08-22 2022-03-22 Novartis Ag Compostos de pirrolopirimidina como inibidores de cdk, bem como composição farmacêutica e combinação
CN102203293A (zh) 2008-10-27 2011-09-28 奇亚根盖瑟斯堡股份有限公司 快速结果杂交捕获测定和系统
KR20120046018A (ko) 2010-10-04 2012-05-09 삼성테크윈 주식회사 단일 뉴클레오티드 다형성의 실시간 pcr 검출
WO2012125848A2 (en) 2011-03-16 2012-09-20 Baylor College Of Medicine A method for comprehensive sequence analysis using deep sequencing technology

Similar Documents

Publication Publication Date Title
JP2017502013A5 (cg-RX-API-DMAC7.html)
JP2017502017A5 (cg-RX-API-DMAC7.html)
JP2017502016A5 (cg-RX-API-DMAC7.html)
JP2017500320A5 (cg-RX-API-DMAC7.html)
RU2016129287A (ru) Лечение злокачественных опухолей с применением комбинаций ингибиторов erk и raf
Gutteridge et al. Plk1 inhibitors in cancer therapy: from laboratory to clinics
Linch et al. Systemic treatment of soft-tissue sarcoma—gold standard and novel therapies
Garcia del Muro et al. A phase II trial of temozolomide as a 6‐week, continuous, oral schedule in patients with advanced soft tissue sarcoma: A study by the Spanish Group for Research on Sarcomas
Nonnenmacher et al. RIST: A potent new combination therapy for glioblastoma
JP2017502014A5 (cg-RX-API-DMAC7.html)
Yesilkanal et al. New strategies for targeting kinase networks in cancer
RU2717570C2 (ru) Синергистические комбинации ауристана
Bailón-Moscoso et al. Development of anticancer drugs based on the hallmarks of tumor cells
Lindauer et al. Dasatinib
O’Sullivan Overcoming endocrine resistance in hormone-receptor positive advanced breast cancer-the emerging role of CDK4/6 inhibitors
EP3442529B1 (en) Combination therapy with notch and cdk4/6 inhibitors for the treatment of lung cancer
Rao et al. Axitinib sensitization of high single dose radiotherapy
EA201200560A1 (ru) Специфическая терапия, использующая интегриновые лиганды для лечения рака
JP2015526410A5 (cg-RX-API-DMAC7.html)
RU2017102319A (ru) Прерывистое введение ингибитора mdm2
MX2014002471A (es) Combinaciones sinergicas de los inhibidores de p13k y mek.
BR112014027010A2 (pt) uso de laquinimod de alta dose para tratamento de esclerose múltipla
Tsai et al. S onic H edgehog inhibition as a strategy to augment radiosensitivity of hepatocellular carcinoma
CA2939464A1 (en) Use of anti-ccr5 antibodies in graft versus host disease
EP4520398A3 (en) Treatment of prostate cancer